Canonical Allele Identifier: CA1339335248

Gene: AGXT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240877088C= , CM000664.2:g.240877088C=	GRCh38
NC_000002.11:g.241816505C= , CM000664.1:g.241816505C=	GRCh37
NC_000002.10:g.241465178C=	NCBI36
NG_008005.1:g.13344C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.847-449C= MANE Select	ENSP00000302620.3:n.847-449C=
ENST00000307503.3:c.847-449C=	ENSP00000302620.3:n.847-449C=
ENST00000470255.1:n.176C=
NM_000030.2:c.847-449C=	NP_000021.1:n.847-449C=
NM_000030.3:c.847-449C= MANE Select	NP_000021.1:n.847-449C=